Canonical Allele Identifier: PA645399090
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411386
ClinVar RCV Id: RCV000561099 RCV000758725 RCV004001931 RCV003651848 RCV002526443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp989Gly
CA034127
NM_001127510.3:c.2966A>G